HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor

Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphoc...

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Veröffentlicht in:Journal of immunotherapy 2009-09, Vol.32 (7), p.755-764
Hauptverfasser: SUNDIN, Mikael, BARRETTE, A. John, RINGDEN, Olle, UZUNEL, Mehmet, LINNIES, Helena, DACKLAND, Asa-Lena, CHRISTENSSON, Birger, LE BLANC, Katarina
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container_end_page 764
container_issue 7
container_start_page 755
container_title Journal of immunotherapy
container_volume 32
creator SUNDIN, Mikael
BARRETTE, A. John
RINGDEN, Olle
UZUNEL, Mehmet
LINNIES, Helena
DACKLAND, Asa-Lena
CHRISTENSSON, Birger
LE BLANC, Katarina
description Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphocyte response to MSC and peripheral blood lymphocytes (PBL) from the MSC or third party donors was measured before and after infusion. In vitro primary and rechallenge lymphocyte responses of healthy individuals to MSC and to PBL from the MSC donor were similarly studied. HSCT recipients given MSC responded to third party allostimuli, but showed no response to infused MSC before and upto 6 months after infusion, whereas maintaining an alloresponse to the MSC donor. This indicates immune unresponsiveness restricted to MSC, as the HSCT recipient was not tolerized to the MSC donor. In vitro, we confirmed that MSC failed to prime responder lymphocytes to rechallenge with PBL from the MSC donor, and lymphocytes primed with MSC donor and rechallenged with MSC only showed weak responses at high stimulator-responder ratios. Although MSC up-regulated lymphocyte gene expression of CD25, IFN-gamma, FoxP3, CTLA-4, and IL-10, they failed in both unprimed and primed responders to induce CD25+ (activated) or CD57+ (effector) CD4+ or CD8+ T-lymphocyte subsets and only inconsistently induced FoxP3+ regulatory T-lymphocytes. These results show for the first time that infused MSC are only weakly immunogenic in humans and validate the clinical use of MSC from HLA-mismatched donors.
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subjects Adolescent
Adult
Antineoplastic agents
Biological and medical sciences
CD8-Positive T-Lymphocytes - cytology
CD8-Positive T-Lymphocytes - immunology
CD8-Positive T-Lymphocytes - metabolism
Child
Female
Flow Cytometry
Gene Expression
Graft vs Host Disease - immunology
Hematopoietic Stem Cell Transplantation
Histocompatibility Testing
Humans
Immunotherapy
Infant
Male
Medical sciences
Mesenchymal Stem Cell Transplantation
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - immunology
Middle Aged
Multipotent Stem Cells - cytology
Multipotent Stem Cells - immunology
Pharmacology. Drug treatments
Reverse Transcriptase Polymerase Chain Reaction
T-Lymphocytes - cytology
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
T-Lymphocytes, Regulatory - cytology
T-Lymphocytes, Regulatory - immunology
T-Lymphocytes, Regulatory - metabolism
Tissue Donors
Transplantation Tolerance - immunology
Young Adult
title HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor
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